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Odor identification predicts the transition of patients with isolated RBD: A retrospective study
INTRODUCTION: To determine if the severity of olfactory dysfunction in isolated REM sleep behavior disorder (IRBD) predicts conversion to Parkinson's disease (PD) or dementia with Lewy bodies (DLB). METHODS: Olfaction was tested using the Japanese version of the University of Pennsylvania Smell...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380141/ https://www.ncbi.nlm.nih.gov/pubmed/35767550 http://dx.doi.org/10.1002/acn3.51615 |
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author | Miyamoto, Tomoyuki Miyamoto, Masayuki |
author_facet | Miyamoto, Tomoyuki Miyamoto, Masayuki |
author_sort | Miyamoto, Tomoyuki |
collection | PubMed |
description | INTRODUCTION: To determine if the severity of olfactory dysfunction in isolated REM sleep behavior disorder (IRBD) predicts conversion to Parkinson's disease (PD) or dementia with Lewy bodies (DLB). METHODS: Olfaction was tested using the Japanese version of the University of Pennsylvania Smell Identification Test (UPSIT‐J) in 155 consecutive patients with polysomnography‐confirmed IRBD and 34 healthy controls. IRBD patients were followed up for 5.8 ± 3.2 (range 0.2–11) years. Thirty‐eight patients underwent repeat UPSIT‐J evaluation at 2.7 ± 1.3 years after the baseline test. RESULTS: UPSIT‐J score was lower in IRBD patients than in age‐ and sex‐matched controls. The receiver operating characteristic curve analysis showed that the optimal cutoff score of 22.5 in UPSIT‐J discriminated between IRBD patients and controls with a sensitivity of 94.3% and specificity of 81.8%. Anosmia (UPSIT‐J score < 19) was present in 54.2% of IRBD patients. In total, 42 patients developed a neurodegenerative disease, of whom 17 had PD, 22 DLB, and 3 MSA. Kaplan–Meier analysis showed that the short‐term risk of Lewy body disease (LBD) was higher in patients with anosmia than in those without anosmia. At baseline, the UPSIT‐J score was similar between patients who developed PD and DLB (p = 0.136). All three IRBD patients (100%) who developed MSA did not have anosmia. CONCLUSIONS: In IRBD patients, anosmia predicts a higher short‐term risk of transition to LBD but cannot distinguish between PD and DLB. At baseline, preserved odor identification may occur in latent MSA. Future IRBD neuroprotective trials should evaluate anosmia as a marker of prodromal LBD. |
format | Online Article Text |
id | pubmed-9380141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93801412022-08-19 Odor identification predicts the transition of patients with isolated RBD: A retrospective study Miyamoto, Tomoyuki Miyamoto, Masayuki Ann Clin Transl Neurol Research Articles INTRODUCTION: To determine if the severity of olfactory dysfunction in isolated REM sleep behavior disorder (IRBD) predicts conversion to Parkinson's disease (PD) or dementia with Lewy bodies (DLB). METHODS: Olfaction was tested using the Japanese version of the University of Pennsylvania Smell Identification Test (UPSIT‐J) in 155 consecutive patients with polysomnography‐confirmed IRBD and 34 healthy controls. IRBD patients were followed up for 5.8 ± 3.2 (range 0.2–11) years. Thirty‐eight patients underwent repeat UPSIT‐J evaluation at 2.7 ± 1.3 years after the baseline test. RESULTS: UPSIT‐J score was lower in IRBD patients than in age‐ and sex‐matched controls. The receiver operating characteristic curve analysis showed that the optimal cutoff score of 22.5 in UPSIT‐J discriminated between IRBD patients and controls with a sensitivity of 94.3% and specificity of 81.8%. Anosmia (UPSIT‐J score < 19) was present in 54.2% of IRBD patients. In total, 42 patients developed a neurodegenerative disease, of whom 17 had PD, 22 DLB, and 3 MSA. Kaplan–Meier analysis showed that the short‐term risk of Lewy body disease (LBD) was higher in patients with anosmia than in those without anosmia. At baseline, the UPSIT‐J score was similar between patients who developed PD and DLB (p = 0.136). All three IRBD patients (100%) who developed MSA did not have anosmia. CONCLUSIONS: In IRBD patients, anosmia predicts a higher short‐term risk of transition to LBD but cannot distinguish between PD and DLB. At baseline, preserved odor identification may occur in latent MSA. Future IRBD neuroprotective trials should evaluate anosmia as a marker of prodromal LBD. John Wiley and Sons Inc. 2022-06-29 /pmc/articles/PMC9380141/ /pubmed/35767550 http://dx.doi.org/10.1002/acn3.51615 Text en © 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Miyamoto, Tomoyuki Miyamoto, Masayuki Odor identification predicts the transition of patients with isolated RBD: A retrospective study |
title | Odor identification predicts the transition of patients with isolated RBD: A retrospective study |
title_full | Odor identification predicts the transition of patients with isolated RBD: A retrospective study |
title_fullStr | Odor identification predicts the transition of patients with isolated RBD: A retrospective study |
title_full_unstemmed | Odor identification predicts the transition of patients with isolated RBD: A retrospective study |
title_short | Odor identification predicts the transition of patients with isolated RBD: A retrospective study |
title_sort | odor identification predicts the transition of patients with isolated rbd: a retrospective study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380141/ https://www.ncbi.nlm.nih.gov/pubmed/35767550 http://dx.doi.org/10.1002/acn3.51615 |
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